Ultrasensitive detection of HIV-1 p24 antigen by a hybrid nanomechanical-optoplasmonic platform with potential for detecting HIV-1 at first week after infection
Early detection of HIV infection is the best way to prevent spread of the disease and to improve the efficiency of the antiretroviral therapy. Nucleic acid amplification tests (NAAT) have become the gold-standard for detecting low-concentrations of the virus in blood. However, these methods are tech...
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description | Early detection of HIV infection is the best way to prevent spread of the disease and to improve the efficiency of the antiretroviral therapy. Nucleic acid amplification tests (NAAT) have become the gold-standard for detecting low-concentrations of the virus in blood. However, these methods are technically demanding and cost-prohibitive in developing countries. Immunoassays are more affordable and can be more easily adapted for point-of-care diagnosis. However, the sensitivity so far of these methods has been too low. We here report the development of a sandwich immunoassay that combines nanomechanical and optoplasmonic transduction methods for detecting the HIV-1 capsid antigen p24 in human serum. The immunoreactions take place on the surface of a compliant microcantilever where gold nanoparticles are used as both mechanical and plasmonic labels. The microcantilever acts as both a mechanical resonator and an optical cavity for the transduction of the mechanical and plasmonic signals. The limit of detection of the immunoassay is 10-17 g/mL that is equivalent to one virion in 10 mL of plasma. This is 5 orders of magnitude better than last generation of approved immunoassays and 2 orders of magnitude better than NAAT. This technology meets the demands to be produced en masse at low cost and the capability for miniaturization to be used at the point-of-care. |
doi_str_mv | 10.1371/journal.pone.0171899 |
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Nucleic acid amplification tests (NAAT) have become the gold-standard for detecting low-concentrations of the virus in blood. However, these methods are technically demanding and cost-prohibitive in developing countries. Immunoassays are more affordable and can be more easily adapted for point-of-care diagnosis. However, the sensitivity so far of these methods has been too low. We here report the development of a sandwich immunoassay that combines nanomechanical and optoplasmonic transduction methods for detecting the HIV-1 capsid antigen p24 in human serum. The immunoreactions take place on the surface of a compliant microcantilever where gold nanoparticles are used as both mechanical and plasmonic labels. The microcantilever acts as both a mechanical resonator and an optical cavity for the transduction of the mechanical and plasmonic signals. The limit of detection of the immunoassay is 10-17 g/mL that is equivalent to one virion in 10 mL of plasma. This is 5 orders of magnitude better than last generation of approved immunoassays and 2 orders of magnitude better than NAAT. This technology meets the demands to be produced en masse at low cost and the capability for miniaturization to be used at the point-of-care.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0171899</identifier><identifier>PMID: 28199410</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Antigens ; Antiretroviral agents ; Antiretroviral therapy ; Arrays ; Biology and Life Sciences ; Biomarkers ; Biosensors ; Cavity resonators ; Developing countries ; Diagnosis ; Engineering and Technology ; Enzymes ; Gold ; Gold - chemistry ; HIV ; HIV Core Protein p24 - blood ; HIV infections ; HIV Infections - diagnosis ; HIV-1 - metabolism ; Human immunodeficiency virus ; Humans ; Immunoassay ; Immunoassay - instrumentation ; Immunoassay - methods ; Immunoassays ; Immunoglobulins ; Infections ; LDCs ; Lentivirus ; Limit of Detection ; Male ; Medicine and Health Sciences ; Metal Nanoparticles - chemistry ; Microscopy ; Miniaturization ; Nanoparticles ; Nanotechnology ; Newton, Isaac (1642-1727) ; p24 Protein ; Physical Sciences ; Point-of-Care Systems ; Research and Analysis Methods ; Retroviridae ; Sensitivity and Specificity ; Virion - chemistry ; Virion - isolation & purification ; Virions ; Viruses</subject><ispartof>PloS one, 2017-02, Vol.12 (2), p.e0171899-e0171899</ispartof><rights>COPYRIGHT 2017 Public Library of Science</rights><rights>2017 Kosaka et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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chemistry</subject><subject>Microscopy</subject><subject>Miniaturization</subject><subject>Nanoparticles</subject><subject>Nanotechnology</subject><subject>Newton, Isaac (1642-1727)</subject><subject>p24 Protein</subject><subject>Physical Sciences</subject><subject>Point-of-Care Systems</subject><subject>Research and Analysis Methods</subject><subject>Retroviridae</subject><subject>Sensitivity and Specificity</subject><subject>Virion - chemistry</subject><subject>Virion - isolation & purification</subject><subject>Virions</subject><subject>Viruses</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqNk99u0zAUxiMEYmPwBggsISG4aPGfxHFukKYJWKVJk4Dt1jqN7dYlsTPb3ejb8Ki4NJtWtIspF7Gd3_nOl3N8iuI1wVPCavJp5dfBQTcdvNNTTGoimuZJcUgaRiecYvb03vqgeBHjCuOKCc6fFwdUkKYpCT4s_lx0KUDULtpkrzVSOuk2We-QN-h0djkhaKAlApfsQjs03yBAy808WIUcON_rdgnOttBN_JD80EHsfd6jvErGhx7d2LREg086K0CH8tltDrcYE0BCxoaY0I3WvxCYpAOyzux8vCyeGeiifjW-j4qLr19-npxOzs6_zU6OzyZtTas04QSIEHOmyqomIFjFjKKK1oYorDlhSgHjzPCKacaJVpozYIJS3oiSN1Sxo-LtTnfofJRjcaMkgguOG1rVmZjtCOVhJYdgewgb6cHKfwc-LCSEZNtOy0orTHFtDKakBGJEKZq5AlCEEZOdZq3PY7b1vNeqzdUJ0O2J7n9xdikX_lpWjGQ3WzMfRoHgr9Y6Jtnb2OquA6f9euu7zk0WnDaPQHmDOa9KkdF3_6EPF2KkFpD_NXfKZ4vtVlQelw2reUUamqnpA1R-lO5tmy-tsfl8L-DjXkBmkv6dFrCOUc5-fH88e365z76_xy41dGkZfbfe3q64D5Y7sA0-xqDNXT8IltuZu62G3M6cHGcuh72538u7oNshY38ByPMniQ</recordid><startdate>20170215</startdate><enddate>20170215</enddate><creator>Kosaka, Priscila M</creator><creator>Pini, Valerio</creator><creator>Calleja, Montserrat</creator><creator>Tamayo, Javier</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20170215</creationdate><title>Ultrasensitive detection of HIV-1 p24 antigen by a hybrid nanomechanical-optoplasmonic platform with potential for detecting HIV-1 at first week after infection</title><author>Kosaka, Priscila M ; Pini, Valerio ; Calleja, Montserrat ; Tamayo, Javier</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c725t-61a188b3d4571a8353fd2d27f1d0e613dda363f653e361ede63a38226984692d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Antigens</topic><topic>Antiretroviral agents</topic><topic>Antiretroviral therapy</topic><topic>Arrays</topic><topic>Biology and Life Sciences</topic><topic>Biomarkers</topic><topic>Biosensors</topic><topic>Cavity resonators</topic><topic>Developing countries</topic><topic>Diagnosis</topic><topic>Engineering and Technology</topic><topic>Enzymes</topic><topic>Gold</topic><topic>Gold - 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Nucleic acid amplification tests (NAAT) have become the gold-standard for detecting low-concentrations of the virus in blood. However, these methods are technically demanding and cost-prohibitive in developing countries. Immunoassays are more affordable and can be more easily adapted for point-of-care diagnosis. However, the sensitivity so far of these methods has been too low. We here report the development of a sandwich immunoassay that combines nanomechanical and optoplasmonic transduction methods for detecting the HIV-1 capsid antigen p24 in human serum. The immunoreactions take place on the surface of a compliant microcantilever where gold nanoparticles are used as both mechanical and plasmonic labels. The microcantilever acts as both a mechanical resonator and an optical cavity for the transduction of the mechanical and plasmonic signals. The limit of detection of the immunoassay is 10-17 g/mL that is equivalent to one virion in 10 mL of plasma. This is 5 orders of magnitude better than last generation of approved immunoassays and 2 orders of magnitude better than NAAT. This technology meets the demands to be produced en masse at low cost and the capability for miniaturization to be used at the point-of-care.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>28199410</pmid><doi>10.1371/journal.pone.0171899</doi><tpages>e0171899</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antigens Antiretroviral agents Antiretroviral therapy Arrays Biology and Life Sciences Biomarkers Biosensors Cavity resonators Developing countries Diagnosis Engineering and Technology Enzymes Gold Gold - chemistry HIV HIV Core Protein p24 - blood HIV infections HIV Infections - diagnosis HIV-1 - metabolism Human immunodeficiency virus Humans Immunoassay Immunoassay - instrumentation Immunoassay - methods Immunoassays Immunoglobulins Infections LDCs Lentivirus Limit of Detection Male Medicine and Health Sciences Metal Nanoparticles - chemistry Microscopy Miniaturization Nanoparticles Nanotechnology Newton, Isaac (1642-1727) p24 Protein Physical Sciences Point-of-Care Systems Research and Analysis Methods Retroviridae Sensitivity and Specificity Virion - chemistry Virion - isolation & purification Virions Viruses |
title | Ultrasensitive detection of HIV-1 p24 antigen by a hybrid nanomechanical-optoplasmonic platform with potential for detecting HIV-1 at first week after infection |
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